Evidence map›Paper›PMID 40759680›Full record

ArticleScientific reports2025

Comparison of Niosomal formulation of citrus limon peel extracts and doxorubicin effects on MCF-7 and MDA-MB-231 human breast cancer cells.

Toktam Deylami, Mohammad Mehdi Yaghoobi, Masoud Torkzadeh-Mahani

Abstract readComparative Study
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Toktam DeylamiDepartment of Biotechnology, Institute of Science and High Technology and Environmental Sciences, Graduate University of Advanced Technology, Kerman, 7631818356, Iran. t.deylami@student.kgut.ac.ir.ORCID http://orcid.org/0000-0001-8184-6929
Mohammad Mehdi YaghoobiDepartment of Biotechnology, Institute of Science and High Technology and Environmental Sciences, Graduate University of Advanced Technology, Kerman, 7631818356, Iran.
Masoud Torkzadeh-MahaniDepartment of Biotechnology, Institute of Science and High Technology and Environmental Sciences, Graduate University of Advanced Technology, Kerman, 7631818356, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Niosome represents a practical approach for targeted the in vitro delivery of phytochemicals and drugs to cells. also it is a promising delivery system for plant extracts and reduces the side effects of burst release of doxorubicin. Ethanolic lemon peel extract (EE), methanolic extract (ME), and doxorubicin (DOXO) were formulated into ethanolic, methanolic, and doxorubicin niosomal formulations, denoted as NIO/EE, NIO/ME, and NIO/DOXO, respectively. These formulations were applied to MCF-7 and MDA-MB-231 breast cancer cell lines for a duration of 48 h. The cells' apoptosis/necrosis and migration rates were measured using Annexin V/PI staining and wound healing assays. Gene expression was measured by qPCR. The results show that NIO/EE and NIO/ME treatments notably elevated the apoptosis rate to unformulated extracts (P < 0.0001). However, NIO/DOXO has significantly milder cytotoxicity than DOXO. The extracts significantly inhibited the migration of both cell lines (P < 0.0001). An increase in FAS expression (****P < 0.0001) and a decreased expression level of VIMENTIN, SNAIL, and JNK-2 genes (***P < 0.001, ****P < 0.0001) is shown in all two cell lines treated with niosomal formulation containing NIO/EE and NIO/ME that confirmed apoptosis induction and migration inhibition by encapsulated extracts. The study aims to evaluate the enhanced anticancer activity usefulness of noisome-encapsulating lemon peel extracts and doxorubicin on breast cancer cells. Further research will reveal the in vivo effects of the extracts in animal models.

Indexed as

Breast NeoplasmsCitrusDoxorubicinPlant ExtractsApoptosisCell Line, TumorCell MovementFemaleHumansLiposomesMCF-7 CellsDoxorubicinLiposomesPlant ExtractsAnti-cancer plantsApoptotic activityCancer therapyCytotoxic effectNiosome formulationSynergistic effects

Identifiers

PMID40759680
PMCPMC12322245

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.